CN112857957A

CN112857957A - Preparation device and preparation method of balance gas in carbonate cluster isotope test

Info

Publication number: CN112857957A
Application number: CN202110020313.3A
Authority: CN
Inventors: 王永生; 胡安平; 沈安江; 佘敏; 王莹
Original assignee: Petrochina Co Ltd
Current assignee: Petrochina Co Ltd
Priority date: 2021-01-07
Filing date: 2021-01-07
Publication date: 2021-05-28
Anticipated expiration: 2041-01-07
Also published as: CN112857957B

Abstract

The invention provides a device and a method for preparing balance gas in a carbonate cluster isotope test. The device includes: at least three carbon dioxide storage devices, at least two condensing devices and a control valve; all the carbon dioxide storage devices are connected in parallel and then are sequentially connected in series with all the condensing devices; a control valve is arranged on a parallel branch of the carbon dioxide storage equipment; a connecting pipeline between the condensing devices is provided with a balance device external branch with a control valve; a series pipeline which is connected in parallel with the carbon dioxide storage devices and is sequentially connected in series with the condensing device is provided with a purification system external branch with a control valve; after being connected in parallel, each carbon dioxide storage device is connected with the condensing device in series in sequence, and a series pipeline is provided with at least one vacuumizing device external branch with a control valve; and after being connected in parallel, the carbon dioxide storage devices are sequentially connected in series with the condensing device, and a series pipeline is provided with a carbon dioxide source external branch with a control valve, or a balance device external branch with a control valve can be connected with the carbon dioxide source.

Description

Preparation device and preparation method of balance gas in carbonate cluster isotope test

Technical Field

The invention belongs to the technical field of analysis and test, and particularly relates to a device and a method for preparing balance gas in carbonate cluster isotope test.

Background

The subject of cluster isotope geochemistry is the isotopic ordering of natural substances, in the 40 s of the 20 th century, hard urea first proposed the hypothesis: two rare isotopes in natural substances have thermodynamic tendencies to combine with each other. Since the abundance of molecules containing two or more rare isotopes is very low, only tens of ppm or even lower, it cannot be detected under the experimental conditions at the time; until the last decade, the sequencing and abundance determination of molecules containing two or more rare isotopes has not been possible due to the upgrading of testing techniques, and cluster isotope technology has evolved. The carbonate cluster isotope is a branch of the application of the cluster isotope on carbonate minerals, and John Eiler of California and a team thereof research and introduce the carbonate cluster isotope from 2004 and establish a framework of the research on the carbonate cluster isotope, so that a solid foundation is laid for the subsequent research on the carbonate cluster isotope. Ghosh first established Delta by applying synthetic calcite in 2006_47-true-T classical calibration curve and finds good application in deep sea corals and corals from the red sea. Carbonate cluster isotope is mainly used for researching carbonate¹³C-¹⁸The abundance of O cannot be directly measured by the current testing technology, and the abundance of O needs to be measured by the acidolysis of carbonate phosphate into carbon dioxide¹³C¹⁸O¹⁶Abundance of O (molecular weight 47), thus expressed as Δ₄₇. In the actual measurement process, due to differences of pretreatment systems, isotope instrument parameter selection and instrument states in various laboratories, data reproducibility among the laboratories is not ideal. In 2011 Dennis first proposed a measured delta for each laboratory based on a method of high temperature gas and equilibrium gas_47-raw(uncorrected) value was normalizedThe data precision and reproducibility are greatly promoted by the aid of the data processing method. However, the requirements for quantification and tightness in the preparation process of the high-temperature gas and water balance gas are high, and the injector is required to pump carbon dioxide gas, so that miscellaneous gas is easy to mix, and the result is inaccurate. Therefore, a novel method for preparing the balance gas in the carbonate cluster isotope test, which is convenient to operate and has high accuracy, is needed, and further development of the cluster isotope test technology is promoted.

Disclosure of Invention

The invention aims to provide a device which is suitable for preparing balance gas in a carbonate cluster isotope test; the device realizes the standardized preparation of the balance gas in the carbonate cluster isotope test, is beneficial to improving the accuracy and precision of a conversion equation established based on the balance gas, further improves the level of the carbonate cluster isotope test technology, and provides reliable support for the carbonate cluster isotope test in the aspect of reconstruction of the ambient temperature.

In order to achieve the above object, the present invention provides an apparatus for preparing an equilibrium gas in a carbonate cluster isotope test, wherein the apparatus comprises:

at least three carbon dioxide storage devices, at least two condensing devices and a control valve; after being connected in parallel, the carbon dioxide storage equipment is sequentially connected with the condensing equipment in series; wherein the content of the first and second substances,

a control valve for controlling the on-off of each branch is arranged on the parallel branch of each carbon dioxide storage device; a connecting pipeline between the condensing devices is provided with a balance device external branch with a control valve, and the external branch is used for realizing the connection with the balance device; a purifying system external branch with a control valve is arranged on a serial pipeline which is connected in series with the condensing equipment in sequence after the carbon dioxide storage equipment is connected in parallel, and the external branch is used for connecting a carbonate cluster isotope testing and purifying system, so that balance gas is conveyed into the carbonate cluster isotope testing and purifying system to carry out a purifying process; a serial pipeline which is connected with the carbon dioxide storage equipment in parallel and then sequentially connected with the condensing equipment in series is provided with at least one external branch of the vacuumizing device with a control valve, and the external branch is used for realizing connection with the vacuumizing device;

wherein, a series pipeline which is connected in series with the condensing equipment in sequence after each carbon dioxide storage equipment is connected in parallel is provided with a carbon dioxide gas source external branch with a control valve, and the external branch is used for realizing the connection with the carbon dioxide gas source; or; the external branch of the balance equipment with the control valve can also be used for realizing the connection with a carbon dioxide gas source.

In the above apparatus for preparing a balance gas in a carbonate cluster isotope test, at least one external branch finger of a vacuum pumping apparatus with a control valve is provided on a serial pipeline which is connected in parallel with each carbon dioxide storage device and then sequentially connected in series with a condensing device: the external branch of the vacuumizing device with the control valve can be arranged on a connecting pipeline between the carbon dioxide storage equipment and the condensing equipment after being connected in parallel, can be arranged on a connecting pipeline between the condensing equipment, can be arranged on a pipeline behind the condensing equipment, and can also be arranged on a pipeline in front of the carbon dioxide storage equipment after being connected in parallel.

In the above apparatus for preparing a balance gas in a carbonate cluster isotope test, a series pipeline, in which the carbon dioxide storage devices are connected in parallel and then connected in series with the condensing device in sequence, is provided with a carbon dioxide gas source external branch finger having a control valve: the carbon dioxide gas source external branch with the control valve can be arranged on a connecting pipeline between the carbon dioxide storage equipment and the condensing equipment after being connected in parallel, can be arranged on a connecting pipeline between the condensing equipment, can be arranged on a pipeline behind the condensing equipment, and can also be arranged on a pipeline in front of the carbon dioxide storage equipment after being connected in parallel.

In the above apparatus for preparing an equilibrium gas in a carbonate cluster isotope test, preferably, the condensing means includes a cold trap and/or a cold finger; in one embodiment, the equilibrium gas preparation device in the carbonate cluster isotope test comprises two condensing devices, namely a cold trap and a cold finger.

In the above apparatus for preparing a balance gas in a carbonate cluster isotope test, preferably, at least two external branches of a vacuum pumping apparatus with control valves are provided on a serial pipeline sequentially connected in series with the condensing apparatus after the carbon dioxide storage apparatuses are connected in parallel, and the external branches are used for realizing connection with the vacuum pumping apparatus; at least one external branch of the vacuumizing device with a control valve is arranged in front of the condensing equipment, and at least one external branch of the vacuumizing device with a control valve is arranged behind the condensing equipment.

In the above apparatus for producing a balanced gas in a carbonate cluster isotope test, it is preferable that the apparatus further includes a pressure gauge provided in a serial line in which the carbon dioxide storage devices are connected in parallel and the condensing device are sequentially connected in series (in other words, the pressure gauge may be provided in a connection line between the carbon dioxide storage devices and the condensing device after being connected in parallel, in a connection line between the condensing devices, in a line after the condensing device, or in a line before the carbon dioxide storage devices after being connected in parallel), and/or in an external branch of a purification system having a control valve. In one embodiment, at least one pressure gauge is located adjacent to the balance apparatus external branch with the control valve to enable determination of the amount of air to and from the balance apparatus connected to the balance apparatus external branch with the control valve. In one embodiment, at least one pressure gauge is disposed adjacent to the carbon dioxide storage device after being connected in parallel, thereby enabling determination of the pressure of the carbon dioxide storage device. The arrangement of the pressure gauge is helpful to realize the quantitative preparation of the balance gas in the carbonate cluster isotope test.

In the above-described balanced gas production apparatus in the carbonate cluster isotope test, preferably, the balanced gas production apparatus in the carbonate cluster isotope test further includes a glass crushing apparatus.

In the above-described balanced gas production apparatus for a carbonate cluster isotope test, preferably, the balanced gas production apparatus for a carbonate cluster isotope test further includes a balancing device, and the balancing device is a glass tube (for example, a quartz tube or a pyrex tube).

In one embodiment, the external branch of the purification system with the control valve is arranged between the condensing devices.

In a specific embodiment, the balance equipment is a quartz tube used for realizing high-temperature gas balance; the balance equipment adopts a pyrex glass tube for realizing water balance and gas balance.

In the above apparatus for preparing the balance gas in the carbonate cluster isotope test, preferably, the pipeline is a glass pipe or a stainless pipe line whose inner wall is polished.

In the above-described balanced gas production apparatus in the carbonate cluster isotope test, it is preferable that the pipes each have a size of 1/4 inches.

In the above apparatus for preparing a balance gas in a carbonate cluster isotope test, preferably, the carbon dioxide storage device is a storage device with a cold finger; in one embodiment, the carbon dioxide storage device is a round bottom flask with a cold finger.

In the above balanced gas preparation apparatus in the carbonate cluster isotope test, preferably, each of the parallel branches of each carbon dioxide storage device is provided with at least two control valves for controlling the on/off of the branch. Carbon dioxide gas stored in a pipeline between the control valves can be used for balancing in the balance gas preparation process, so that quantitative preparation of the balance gas is more facilitated.

In the above apparatus for preparing a balanced gas in a carbonate cluster isotope test, it is preferable that a control valve is provided on a connection line between the carbon dioxide storage device and the condensing device connected in parallel.

In the above apparatus for preparing balanced gas in carbonate cluster isotope test, preferably, a control valve is disposed on a connection pipeline between an external branch of the balancing device with a control valve and a condensing device near the carbon dioxide storage device.

The invention also provides a preparation method of the balance gas in the carbonate cluster isotope test, which is carried out by using the preparation device of the balance gas in the carbonate cluster isotope test, wherein the method comprises the following steps:

1) pure carbon dioxide gas consisting of various carbon isotopes and oxygen isotopes is respectively led into different carbon dioxide storage equipment, so that each pure carbon dioxide gas is independently stored; wherein, the types of the pure carbon dioxide gas are not less than 3; wherein, the introduction of each pure carbon dioxide gas into the carbon dioxide storage device is realized by adopting the following mode:

the gas source and the vacuum pumping equipment of the pure carbon dioxide gas are connected into a balanced gas preparation device in the carbonate cluster isotope test through corresponding external branches; vacuumizing a balance gas preparation device in the carbonate cluster isotope test by using vacuumizing equipment; then the pure carbon dioxide gas is led into the carbon dioxide storage equipment through controlling each control valve;

2) the balance equipment and the vacuumizing equipment are connected into a balance gas preparation device in the carbonate cluster isotope test through corresponding external branches, and different pure carbon dioxide gases stored in the carbon dioxide storage equipment are sequentially introduced into the balance equipment; wherein, each pure carbon dioxide gas is introduced into the balance equipment by adopting the following method:

vacuumizing a balance gas preparation device in the carbonate cluster isotope test by using vacuumizing equipment; then on the basis of controlling each control valve, the pure carbon dioxide gas is sequentially subjected to freezing dehydration and impurity removal by using condensing equipment, and then is introduced into balancing equipment;

wherein, the control valve of the external branch connected with the vacuum pumping equipment is in an open state in the vacuum pumping operation before the pure carbon dioxide gas is introduced into the balance equipment for the first time, and the control valve is in a close state in the vacuum pumping operation before the pure carbon dioxide gas is introduced into the balance equipment for the subsequent time;

3) the balance of each component in the balance equipment is realized at a set temperature;

4) and leading the balanced gas in the balancing equipment out to a carbonate cluster isotope test purification system through an external branch of the purification system with a control valve.

In the above method for preparing the balance gas in the carbonate cluster isotope test, preferably, the step of controlling the control valves, sequentially performing freezing, water removal and impurity removal on the pure carbon dioxide gas by using a condensing device, and then introducing the pure carbon dioxide gas into the balance device comprises:

A. one of the condensing devices is arranged in an environment capable of realizing carbon dioxide solidification, and the pure carbon dioxide gas is introduced into the condensing device and solidified; then, removing impurities by using vacuumizing equipment to pump out impurity gases;

B. setting another new condensing device in an environment capable of realizing carbon dioxide solidification, adjusting the environment of the original condensing device containing the pure carbon dioxide from the environment capable of realizing carbon dioxide solidification to an environment capable of realizing carbon dioxide gasification and maintaining water in a solidification state, transferring the pure carbon dioxide gas into the new condensing device and solidifying, and keeping water in the original condensing device in the carbon dioxide gas transferring process to realize carbon dioxide gas dehydration; then, removing impurities by using vacuumizing equipment to pump out impurity gases;

C. repeating the step B until the pure carbon dioxide gas is transferred to the last condensing equipment and solidified, and then using vacuumizing equipment to pump out impurity gas to remove impurities;

D. the method comprises the following steps of arranging balance equipment in an environment capable of realizing carbon dioxide solidification, adjusting the environment where the last condensing equipment is located from the environment capable of realizing carbon dioxide solidification to an environment capable of realizing carbon dioxide gasification and maintaining water in a solidification state, transferring pure carbon dioxide gas into the balance equipment and solidifying, and enabling water to still remain in the last original condensing equipment in the carbon dioxide gas transferring process to realize carbon dioxide gas dehydration;

more preferably, the last condensing device is a cold finger;

more preferably, in step D, the pressure of the pure carbon dioxide gas transferred to the balancing device is detected by using a pressure gauge pair, so as to determine the amount of the pure carbon dioxide gas transferred to the balancing device.

In the above method for preparing balanced gas in carbonate cluster isotope test, preferably, in step 2), in the process of connecting the balancing apparatus to the balanced gas preparation apparatus in carbonate cluster isotope test through the corresponding external branch, deionized water is already filled in the balancing apparatus, and at this time, the product obtained in step 3) is water balanced gas.

In the above method for preparing balance gas in carbonate cluster isotope test, preferably, the step of guiding the balanced gas in the balance device to the carbonate cluster isotope test purification system through a purification system external branch with a control valve includes:

E. respectively connecting the balance equipment, the vacuumizing equipment and the carbonate cluster isotope test purification system into a balance gas preparation device in the carbonate cluster isotope test through corresponding external branches; vacuumizing a balance gas preparation device in the carbonate cluster isotope test by using vacuumizing equipment under the condition that the balance equipment is in a closed state;

F. one of the condensing devices is arranged in an environment capable of realizing carbon dioxide solidification, the balance device is arranged in an environment capable of realizing carbon dioxide gasification and maintaining water in a solidification state, balance gas is transferred into the condensing device and solidified, and water is still left in the balance device in the balance gas transfer process to realize water removal; then, removing impurities by using vacuumizing equipment to pump out impurity gases;

G. adjusting the environment of the condensing equipment containing the balance gas from the environment capable of realizing carbon dioxide solidification to the environment capable of realizing carbon dioxide gasification and maintaining water in a solidification state, leading the balance gas out to a carbonate cluster isotope test purification system by combining the control of each control valve, and keeping water in the condensing equipment to realize water removal in the process of leading the balance gas out;

more preferably, in step G, the pressure of the balance gas is detected by using a pressure gauge pair during the process of leading the balance gas out to the carbonate cluster isotope testing and purifying system, so as to determine the gas amount of the balance gas led out to the carbonate cluster isotope testing and purifying system.

In the above method for preparing the balanced gas in the carbonate cluster isotope test, preferably, the environment capable of achieving solidification of carbon dioxide is a liquid nitrogen environment.

In the above method for preparing an equilibrium gas in the carbonate cluster isotope test, it is preferable that the environment capable of achieving gasification of carbon dioxide and maintaining water in a solidified state is a mixture environment of methanol and liquid nitrogen at-90 ℃.

In the above method for preparing the balance gas in the carbonate cluster isotope test, preferably, the step 3) of achieving the balance of the components in the balance equipment at the set temperature is achieved by:

sealing the balancing equipment, and standing at a set temperature for a period of time to realize the balance of each component in the balancing equipment;

in a specific embodiment, the set temperature is one of 1000 ℃, 50 ℃ and 15 ℃;

in a specific embodiment, the set period of time is not less than 2 hours.

In the above method for preparing the balance gas in the carbonate cluster isotope test, the pure carbon dioxide gas composed of various carbon isotopes and oxygen isotopes is selected from the pure carbon dioxide gas species commonly used for preparing the balance gas in the carbonate cluster isotope test; in one embodiment, the pure carbon dioxide gas with different carbon and oxygen isotopes comprises at least three of carbon dioxide gas with carbon atom content of-33.5 permillage (VPDB), carbon dioxide gas with carbon atom content of-15.6 permillage (VPDB), carbon dioxide gas with carbon atom content of-20.6 permillage (VPDB), carbon dioxide gas with carbon atom content of-8.4 permillage (VPDB), carbon dioxide gas with carbon atom content of-8.6 permillage (VPDB), carbon dioxide gas with carbon atom content of-4.3 permillage (VPDB), and carbon dioxide gas with carbon atom content of-1.5 permillage (VPDB) and carbon dioxide gas with carbon atom content of 1.5 permillage (VPDB).

The inventor provides a brand-new balanced gas preparation device in the carbonate cluster isotope test, which can effectively reduce the doping of miscellaneous gas, water vapor and the like and improve the purity of the prepared balanced gas, from the viewpoints of realizing the process and standardization of the preparation of the balanced gas in the carbonate cluster isotope test and improving the reproducibility and precision of the data of the balanced gas. The method for preparing the balance gas based on the brand-new device for preparing the balance gas in the carbonate cluster isotope test provided by the invention obviously improves the accuracy and precision of a conversion equation established based on the balance gas, further improves the level of a carbonate cluster isotope test technology, and provides reliable support for the reconstruction of the technology at the ambient temperature.

Drawings

Fig. 1 is a schematic diagram of the preparation of the equilibrium gas in the carbonate cluster isotope test provided in example 1 of the present invention.

Description of the main reference numerals:

1. 2, 3 and 4 round-bottom flasks with cold fingers, V1, V2-1-1, V2-1-2, V2-2-1, V2-2-2, V2-3-1, V2-3-2, V2-4-1, V2-4-2, V3, V4, V5, V6, V7, V8 and V9 control valves, P1 and P2 pressure gauges, S2U-shaped cold traps, S4 cold fingers are connected in series, S3, S5, S6 and S7 are connected with an external branch, a C1 glass breaking device and a C2 balancing device.

Detailed Description

In order to make the objects, technical solutions and advantages of the embodiments of the present invention clearer, the technical solutions in the embodiments of the present invention will be described in detail and completely with reference to the drawings in the embodiments of the present invention. It is to be understood that the embodiments described are only a few embodiments of the present invention, and not all embodiments. All other embodiments, which can be derived by a person skilled in the art from the embodiments given herein without making any creative effort, shall fall within the protection scope of the present invention.

Example 1

The embodiment of the invention provides a balanced gas preparation device in a carbonate cluster isotope test, as shown in fig. 1, the device comprises:

4 carbon dioxide storage devices, 2 condensing devices, 16 control valves, 2 pressure gauges and connecting pipelines; wherein, the 4 carbon dioxide storage devices are respectively a round-bottom flask 1 with a cold finger, a round-bottom flask 2 with a cold finger, a round-bottom flask 3 with a cold finger and a round-bottom flask 4 with a cold finger; the 2 condensing devices are respectively a U-shaped cold trap S2 and a cold finger S4; the 16 control valve ratio is divided into a control valve V1, a control valve V2-1-1, a control valve V2-1-2, a control valve V2-2-1, a control valve V2-2-2, a control valve V2-3-1, a control valve V2-3-2, a control valve V2-4-1, a control valve V2-4-2, a control valve V3, a control valve V4, a control valve V5, a control valve V6, a control valve V7, a control valve V8 and a control valve V9; the 2 pressure gauges are respectively a pressure gauge P1 and a pressure gauge P2;

a round-bottom flask 1 with a cold finger, a round-bottom flask 2 with a cold finger, a round-bottom flask 3 with a cold finger and a round-bottom flask 4 with a cold finger are connected in parallel and then are connected with a U-shaped cold trap S2 and a cold finger S4 in series;

round bottom flask with cold fingers 1, round bottom flask with cold fingers 2, round bottom flask with cold fingers 3 and round bottom flask with cold fingers 4 are connected in parallel to form 4 branches respectively: a round bottom flask with a cold finger 1 branch, a round bottom flask with a cold finger 2 branch, a round bottom flask with a cold finger 3 branch and a round bottom flask with a cold finger 3 branch; a branch of the round-bottom flask 1 with the cold fingers is provided with a control valve V2-1-1 and a control valve V2-1-2; a branch of the round-bottom flask 2 with the cold fingers is provided with a control valve V2-2-1 and a control valve V2-2-2; a branch of the round-bottom flask 3 with the cold fingers is provided with a control valve V2-3-1 and a control valve V2-3-2; a control valve V2-4-1 and a control valve V2-4-2 are arranged on a branch of the round-bottom flask 4 with the cold fingers;

a round-bottom flask 1 with a cold finger, a round-bottom flask 2 with a cold finger, a round-bottom flask 3 with a cold finger and a round-bottom flask 4 with a cold finger are connected in parallel, and then are sequentially provided with a control valve V3, a pressure gauge P1, a carbon dioxide gas source external branch S1 with a control valve V9 and a vacuumizing device external branch S5 with a control valve V4 on a connecting pipeline between the U-shaped cold trap S2;

a connecting pipeline between the U-shaped cold trap S2 and the cold finger S4 is sequentially provided with a control valve V5, a purification system external branch S6 with a control valve V6 and a balance equipment external branch S3 with a control valve V7; a pressure gauge P2 is arranged on an external branch S6 of the purification system with a control valve V6;

an external branch S7 of the vacuum extractor with a control valve V8 is arranged on a pipeline behind the cold finger S4;

a control valve V1 is arranged on a pipeline in front of the round-bottom flask 1 with the cold fingers, the round-bottom flask 2 with the cold fingers, the round-bottom flask 3 with the cold fingers and the round-bottom flask with the cold fingers which are connected in parallel;

further, the balance gas preparation device in the carbonate cluster isotope test comprises balance equipment C2, specifically comprising water balance gas balance equipment and high-temperature gas balance equipment; wherein, the water balance gas balance equipment is a pyrex glass tube, and the high-temperature gas balance equipment is a quartz tube;

further, the balance gas preparation device in the carbonate cluster isotope test comprises a glass crushing device C1 used for carrying out C2 seal crushing on balance equipment;

furthermore, a pipeline used by the balance gas preparation device in the carbonate cluster isotope test is a stainless pipe pipeline with the inner wall polished; the dimensions of the pipes are 1/4 inches;

further, the volumes of cold finger round bottom flask 1, cold finger round bottom flask 2, cold finger round bottom flask 3 and cold finger round bottom flask 4 were all 2000 mL.

Example 2

The embodiment of the invention provides a method for preparing balance gas in a carbonate cluster isotope test, which is carried out by using the device for preparing balance gas in the carbonate cluster isotope test provided in the embodiment 1, and comprises the following steps:

s100, respectively introducing pure carbon dioxide gas (such as carbon dioxide gas with carbon and oxygen isotopes of-33.5 thousandths (VPDB), carbon dioxide gas with oxygen isotopes of-15.6 thousandths (VPDB), carbon dioxide gas with carbon and oxygen isotopes of-20.6 thousandths (VPDB), carbon dioxide gas with oxygen isotopes of-8.4 thousandths (VPDB), carbon dioxide gas with carbon and oxygen isotopes of-8.6 thousandths (VPDB), carbon dioxide gas with carbon and oxygen isotopes of-4.3 thousandths (VPDB), carbon dioxide gas with carbon and oxygen isotopes of-1.5 thousandths (VPDB) and O:1.5 thousandths (VPDB)) into a round bottom flask 1 with a cold finger, a round bottom flask 2 with a cold finger, a round bottom flask 3 with a cold finger and a round bottom flask 4 with a cold finger, so as to realize independent storage of each pure carbon dioxide gas; wherein, the types of the pure carbon dioxide gas are 4; wherein the introduction of each pure carbon dioxide gas into the carbon dioxide storage facility is performed in the same manner, taking as an example the introduction of a certain pure carbon dioxide gas into a round bottom flask 1 with cold fingers:

s110, connecting a 1L pure carbon dioxide storage small steel cylinder with a pressure reducing valve to a process through an external branch S1, connecting low-vacuum pumping equipment to the process through an external branch S5, and connecting high-vacuum pumping equipment to the process through an external branch S7;

wherein, the 1L pure carbon dioxide storage small steel cylinder with the pressure reducing valve is preferably connected with an external branch S1 through a quick connector ultra-torr;

after a 1L pure carbon dioxide storage small steel cylinder with a pressure reducing valve, low vacuum vacuumizing equipment and high vacuum vacuumizing equipment are connected, preferably checking the flow tightness;

wherein, the pressure reducing valve preferably adjusts the output pressure to be below 0.2 Mpa;

s120, vacuumizing the whole process: firstly, further closing a control valve V1, a control valve V6, a control valve V7 and a control valve V8, opening the control valve V3, a control valve V2-1-1, a control valve V2-1-2, a control valve V2-2-1, a control valve V2-2-2, a control valve V2-3-1, a control valve V2-3-2, a control valve V2-4-1, a control valve V2-4-2, a control valve V4, a control valve V5 and a control valve V9 under the closing state of a pressure reducing valve of the steel cylinder, and vacuumizing by using low vacuum vacuumizing equipment; when the vacuum is reduced to 10^-2After mbar (i.e. pressure gauge P1, pressure gauge P2 both show 10^-2mbar), the control valve V4 is closed, the control valve V8 is opened, and the vacuum is pumped to 10 by using a high vacuum pumping device^-6mbar (i.e. pressure gauges P1, P2 both show 10^-6mbar) is continuously pumped for more than 30 minutes under the vacuum condition, so that the gas in the pipeline is ensured to be pumped completely; then closing control valve V2-2-1, control valve V2-2-2, control valve V2-3-1, control valve V2-3-2, control valve V2-4-1, control valve V2-4-2, control valve V5, control valve V8 (when introducing a certain pure carbon dioxide gas into round bottom flask 2 with cold fingers, only the differences are that control valve V2-1-1, control valve V2-1-2 are closed, control valve V2-2-1 and control valve V2-2-2 are not closed, when introducing a certain pure carbon dioxide gas into round bottom flask 3 with cold fingers, only the differences are that control valve V2-1-1, control valve V2-1-2 are closed, control valve V2-3-1 and control valve V2-3-2 are not closed, and when introducing a certain pure carbon dioxide gas into round bottom flask 3 with cold fingers When the bottle 4 is used, the difference is only that the control valve V2-1-1 and the control valve V2-1-2 are closed, and the control valve V2-4-1 and the control valve V2-4-2 are not closed);

s130, filling pure CO into round-bottom flask 1 with cold fingers₂Gas: adjusting the pressure reducing valve of the small steel cylinder to 0.2Mpa, opening the pressure reducing valve to charge gas into the round-bottom flask 1 with the cold finger, displaying the accurate pressure of the gas through a pressure gauge P1, and closing a control valve V2-1-1 and a control valve V2-1-2 after the gas is charged;

among them, when the amount of the gas to be introduced into the round-bottomed flask with a cold finger is 2000mL, the aeration time is preferably 5 minutes.

S200, connecting a pyrex glass tube with an opening at one end and filled with deionized water required for preparing water balance gas to the process through an external branch S3, connecting low-vacuum equipment to the process through an external branch S5, and connecting high-vacuum equipment to the process through an external branch S7; wherein, the size of the pyrex glass tube is preferably about 23cm in length, 6mm in outer diameter and 3mm in inner diameter; wherein, the pyrex glass tube is preferably connected with the external branch S3 through a fast interface ultra-torr; wherein the amount of the deionized water is preferably 3.5 mL;

then introducing pure carbon dioxide gas stored in a round-bottom flask 1 with a cold finger, a round-bottom flask 2 with a cold finger, a round-bottom flask 3 with a cold finger and a round-bottom flask 4 with a cold finger into a pyrex glass tube in sequence, wherein the steps specifically comprise:

s210, introducing pure carbon dioxide gas stored in the round-bottom flask 1 with the cold fingers into a pyrex glass tube in sequence:

1) vacuumizing the whole system: putting a pyrex glass tube on a mixture of methanol and liquid nitrogen at the temperature of-90 ℃, and opening a control valve V3, a control valve V4, a control valve V5, a control valve V7, closing the control valve V1, a control valve V2-1-1, a control valve V2-1-2, a control valve V2-2-1, a control valve V2-2-2, a control valve V2-3-1, a control valve V2-3-2, a control valve V2-4-1, a control valve V2-4-2, a control valve V6, a control valve V8 and a control valve V9; by means of a control valve V₄Vacuumizing the connected low-vacuum vacuumizing equipment until the vacuum is reduced to 10^-2mbar closes the control valve V4, and high vacuum equipment connected with the control valve V8 is started to vacuumize to 10^-6mbar, continuously pumping for more than 30 minutes under the vacuum condition to ensure that the vacuum of the pipeline is clean; closing the control valve V7, and removing the mixture of methanol and liquid nitrogen at-90 ℃ on the pyrex glass pipe sleeve;

2) gas transfer: then closing control valve V5 and control valve V8, sleeving liquid nitrogen on the position of U-shaped cold trap S2, opening control valve V2-1-1 on round-bottom flask 1 with cold fingers, closing control valve V2-1-1 after a period of time (preferably about 3 seconds), and opening control valve V2-1-2(ii) a CO between control valve V2-1-1 and control valve V2-1-2₂The gas is transferred into a U-shaped cold trap S2 due to temperature difference, and the whole transfer time is about 5 minutes; ensuring pipeline CO₂After all the gas is absorbed, opening the control valve V5 and the control valve V8, pumping out impurity gas by using high-vacuum pumping equipment, and closing the control valve V5 and the control valve V8 after a period of time (about 2 minutes later); then covering liquid nitrogen on the cold finger S4, replacing the liquid nitrogen on the U-shaped cold trap S2 position sleeve with a mixture of methanol and liquid nitrogen at the temperature of-90 ℃ (note: analytical pure methanol is continuously added into the liquid nitrogen, stirring is carried out while adding, temperature is measured by temperature and temperature is adjusted to-90 ℃), a control valve V5 is opened, and CO is measured by a temperature sensor₂Transferring the gas from the U-shaped cold trap S2 to the cold finger S4, and keeping water in the U-shaped cold trap S2 to remove water in the carbon dioxide gas, closing the control valve V5 after the transfer is finished, and removing a mixture of methanol and liquid nitrogen at the temperature of-90 ℃ in the U-shaped cold trap S2; the liquid nitrogen in the cold finger S4 was changed to a mixture of methanol and liquid nitrogen at-90 deg.C, and the CO was read by a display instrument P2₂The amount of gas was measured, then the Pyrex glass tube was covered with liquid nitrogen to immerse the Pyrex glass tube in the liquid nitrogen and the control valve V7 was opened for 3 minutes, CO₂The gas was transferred from cold finger S4 to pyrex glass tube via line;

s220, introducing pure carbon dioxide gas stored in the round-bottom flask 2 with the cold fingers into a pyrex glass tube in sequence:

1) vacuumizing the whole system: by opening a control valve V3, a control valve V4 and a control valve V5, closing the control valve V1, the control valve V2-1-1, the control valve V2-1-2, the control valve V2-2-1, the control valve V2-2-2, the control valve V2-3-1, the control valve V2-3-2, the control valve V2-4-1, the control valve V2-4-2, the control valve V6, the control valve V8, the control valve V9 and the control valve V7; by means of a control valve V₄Vacuumizing the connected low-vacuum vacuumizing equipment until the vacuum is reduced to 10^-2mbar closes the control valve V4, and high vacuum equipment connected with the control valve V8 is started to vacuumize to 10^-6mbar, continuously pumping for more than 30 minutes under the vacuum condition to ensure that the vacuum of the pipeline is clean;

2) gas transfer: then, the control valve V5 and the control valve V8 are closed, liquid nitrogen is sleeved on the U-shaped cold trap S2, and the belt is openedA control valve V2-2-1 on the round bottom flask 2 with a cold finger is closed after a period of time (preferably about 3 seconds), and a control valve V2-2-1 is opened, and a control valve V2-2-2 is opened; CO between control valve V2-2-1 and control valve V2-2-2₂The gas is transferred into a U-shaped cold trap S2 due to temperature difference, and the whole transfer time is about 5 minutes; ensuring pipeline CO₂After all the gas is absorbed, opening the control valve V5 and the control valve V8, pumping out impurity gas by using high-vacuum pumping equipment, and closing the control valve V5 and the control valve V8 after a period of time (about 2 minutes later); then covering liquid nitrogen on the cold finger S4, replacing the liquid nitrogen on the U-shaped cold trap S2 position sleeve with a mixture of methanol and liquid nitrogen at the temperature of-90 ℃ (note: analytical pure methanol is continuously added into the liquid nitrogen, stirring is carried out while adding, temperature is measured by temperature and temperature is adjusted to-90 ℃), a control valve V5 is opened, and CO is measured by a temperature sensor₂Transferring the gas from the U-shaped cold trap S2 to the cold finger S4, and keeping water in the U-shaped cold trap S2 to remove water in the carbon dioxide gas, closing the control valve V5 after the transfer is finished, and removing a mixture of methanol and liquid nitrogen at the temperature of-90 ℃ in the U-shaped cold trap S2; the liquid nitrogen in the cold finger S4 was changed to a mixture of methanol and liquid nitrogen at-90 deg.C, and the CO was read by a display instrument P2₂The amount of gas was measured, then the Pyrex glass tube was covered with liquid nitrogen to immerse the Pyrex glass tube in the liquid nitrogen and the control valve V7 was opened for 3 minutes, CO₂The gas was transferred from cold finger S4 to pyrex glass tube via line;

s230, repeating the step S220 to respectively guide pure carbon dioxide gas stored in the round-bottom flask 3 with the cold fingers and the round-bottom flask 4 with the cold fingers into the pyrex glass tube in sequence;

the difference is that when pure carbon dioxide gas stored in the round-bottom flask 3 with the cold fingers is sequentially introduced into the pyrex glass tube, in the step 2), liquid nitrogen is sleeved on the position of the U-shaped cold trap S2, the control valve V2-3-1 on the round-bottom flask 3 with the cold fingers is opened (instead of opening the control valve V2-2-1 on the round-bottom flask 2 with the cold fingers), the control valve V2-3-1 (and the control valve V2-2-1) is closed after a period of time (preferably about 3 seconds), and the control valve V2-3-2 is opened; CO between the control valve V2-3-1 and the control valve V2-3-2 (instead of between the control valve V2-2-1 and the control valve V2-2-2)₂Gas transfer to U-shaped cold trap S2 due to temperature differenceThe total transfer time is about 5 minutes;

when pure carbon dioxide gas stored in the round-bottomed flask 4 with the cold fingers is sequentially introduced into the pyrex glass tubes, in the step 2), liquid nitrogen is sleeved at the position of a U-shaped cold trap S2, a control valve V2-4-1 on the round-bottomed flask 4 with the cold fingers is opened (instead of opening a control valve V2-2-1 on the round-bottomed flask 2 with the cold fingers), the control valve V2-4-1 (and the control valve V2-2-1) is closed after a period of time (preferably about 3 seconds), and the control valve V2-3-2 is opened; CO between the control valve V2-4-1 and the control valve V2-4-2 (rather than between the control valve V2-2-1 and the control valve V2-2-2)₂The gas is transferred into a U-shaped cold trap S2 due to temperature difference, and the whole transfer time is about 5 minutes;

s240, sealing the upper end of the pyrex glass tube by high-temperature fusion by using high-temperature flame (for example, more than 1000 ℃);

the high temperature flame is preferably prepared by mixing propane and oxygen, and adjusting the gas flow rate respectively by a cutting gun to control the flame temperature to be more than 1000 ℃.

S300, balancing gas:

sealing the container with deionized water and CO₂The pyrex glass tube is placed in a water bath with adjusted temperature (e.g. 50 deg.C, 25 deg.C, etc.) and H is used₂O-CO₂Oxygen isotope exchange is carried out, and the solution is taken out to be tested after 2 to 3 days of balance (preferably 3 days of balance);

s400, purifying in a pretreatment process of the well-balanced gas-implanted cluster isotope:

s410, connecting a pyrex glass tube with the following process: the glass breaking device (Cracker) C1 was connected to the process via an external branch S3, and H was connected to the process₂O-CO₂The balanced pyrex glass tube is connected to a glass crushing device C1, the low-vacuum vacuumizing equipment is connected to the process through an external branch S5, and the high-vacuum vacuumizing equipment is connected to the process through an external branch S7; wherein the pyrex glass tube is not broken for the time being;

s420, vacuumizing the whole system: under the condition that the pyrex glass tube is not broken for a while, the control valve V is closed₃Control valve V₆Control valve V₈Control valve V₉Opening the control valve V₄Control valve V₅Control valve V₇Vacuumizing by using low-vacuum vacuumizing equipment until the vacuum is reduced to 10^-2mbar cut-off control valve V₄Starting the control valve V₈The connected high vacuum-pumping equipment is vacuumized to 10^-6mbar；

S430, gas transfer: closing the control valve V₅Control valve V₈Breaking the seal of pyrex glass tube with glass breaking device, covering cold finger S4 with liquid nitrogen, covering pyrex glass tube with-90 deg.C mixture of methanol and liquid nitrogen, and CO in pyrex glass tube₂Transferring to a cold finger S4, and opening a control valve V after the transfer is completed₈Removing the miscellaneous gases, and then closing the control valve V₇Control valve V₈The liquid nitrogen on the cold finger S4 sleeve is changed into a mixture of methanol and liquid nitrogen at the temperature of-90 ℃, and CO is read by a pressure display instrument P2₂The amount of gas, and then the control valve V₆CO in cold finger S4₂The gas is transferred to the purification process of cluster gas, and the purified clean CO is obtained₂Collecting gas with special gas collecting bottle, injecting sample via two-way system of Mat-253, and testing delta_47-rawValue, here not expanded.

Example 3

s120, vacuumizing the whole process: firstly, further closing a control valve V1, a control valve V6, a control valve V7 and a control valve V8, opening the control valve V3, a control valve V2-1-1, a control valve V2-1-2, a control valve V2-2-1, a control valve V2-2-2, a control valve V2-3-1, a control valve V2-3-2, a control valve V2-4-1, a control valve V2-4-2, a control valve V4, a control valve V5 and a control valve V9 under the closing state of a pressure reducing valve of the steel cylinder, and vacuumizing by using low vacuum vacuumizing equipment; when the vacuum is reduced to 10^-2After mbar (i.e. pressure gauge P1, pressure gauge P2 both show 10^-2mbar), the control valve V4 is closed, the control valve V8 is opened, and the vacuum is pumped to 10 by using a high vacuum pumping device^-6mbar (i.e. pressure gauges P1, P2 both show 10^-6mbar) is continuously pumped for more than 30 minutes under the vacuum condition, so that the gas in the pipeline is ensured to be pumped completely; then closing control valve V2-2-1, control valve V2-2-2, control valve V2-3-1, control valve V2-3-2, control valve V2-4-1, control valve V2-4-2, control valve V5 and control valve V8 (when introducing certain pure carbon dioxide gas into round bottom flask 2 with cold fingers, the difference is only closing control valve V2-1-1, control valve V2-1-2, and not closing control valve V2-2-1 and control valve V2-2-2; when introducing certain pure carbon dioxide gas into round bottom flask 2 with cold fingersWhen referring to the round-bottom flask 3, the difference is only that the control valve V2-1-1 and the control valve V2-1-2 are closed, and the control valve V2-3-1 and the control valve V2-3-2 are not closed; when a certain pure carbon dioxide gas was introduced into round-bottomed flask 4 with cold fingers, the only difference was that control valve V2-1-1, control valve V2-1-2 were closed, and control valve V2-4-1, control valve V2-4-2 were not closed);

S200, connecting a quartz glass tube with an opening at one end to a process through an external branch S3, connecting low-vacuum equipment to the process through an external branch S5, and connecting high-vacuum equipment to the process through an external branch S7; wherein, the quartz glass tube preferably has the size of about 23cm in length, 6mm in outer diameter and 3mm in inner diameter; wherein, the quartz glass tube is preferably connected with the external branch S3 through a quick interface ultra-torr;

then introducing pure carbon dioxide gas stored in a round-bottom flask 1 with a cold finger, a round-bottom flask 2 with a cold finger, a round-bottom flask 3 with a cold finger and a round-bottom flask 4 with a cold finger into a quartz glass tube in sequence, wherein the steps specifically comprise:

s210, introducing pure carbon dioxide gas stored in the round-bottom flask 1 with the cold fingers into a quartz glass tube in sequence:

1) vacuumizing the whole system: by opening a control valve V3, a control valve V4, a control valve V5 and a control valve V7, closing a control valve V1, a control valve V2-1-1, a control valve V2-1-2, a control valve V2-2-1, a control valve V2-2-2, a control valve V2-3-1, a control valve V2-3-2, a control valve V2-4-1, a control valve V2-4-2, a control valve V6, a control valve V8 and a control valve V9; by means of a control valve V₄Vacuumizing the connected low-vacuum vacuumizing equipment until the vacuum is reduced to 10^-2mbar closes the control valve V4, and high vacuum equipment connected with the control valve V8 is started to vacuumize to 10^-6mbar inContinuously pumping for more than 30 minutes under the vacuum condition to ensure that the pipeline is vacuum and clean;

2) gas transfer: then closing a control valve V5 and a control valve V8, sleeving liquid nitrogen at the position of a U-shaped cold trap S2, opening a control valve V2-1-1 on a round-bottom flask 1 with cold fingers, closing the control valve V2-1-1 after a period of time (preferably about 3 seconds), and opening a control valve V2-1-2; CO between control valve V2-1-1 and control valve V2-1-2₂The gas is transferred into a U-shaped cold trap S2 due to temperature difference, and the whole transfer time is about 5 minutes; ensuring pipeline CO₂After all the gas is absorbed, opening the control valve V5 and the control valve V8, pumping out impurity gas by using high-vacuum pumping equipment, and closing the control valve V5 and the control valve V8 after a period of time (about 2 minutes later); then covering liquid nitrogen on the cold finger S4, replacing the liquid nitrogen on the U-shaped cold trap S2 position sleeve with a mixture of methanol and liquid nitrogen at the temperature of-90 ℃ (note: analytical pure methanol is continuously added into the liquid nitrogen, stirring is carried out while adding, temperature is measured by temperature and temperature is adjusted to-90 ℃), a control valve V5 is opened, and CO is measured by a temperature sensor₂Transferring the gas from the U-shaped cold trap S2 to the cold finger S4, and keeping water in the U-shaped cold trap S2 to remove water in the carbon dioxide gas, closing the control valve V5 after the transfer is finished, and removing a mixture of methanol and liquid nitrogen at the temperature of-90 ℃ in the U-shaped cold trap S2; the liquid nitrogen in the cold finger S4 was changed to a mixture of methanol and liquid nitrogen at-90 deg.C, and the CO was read by a display instrument P2₂The amount of gas was measured, and then the quartz glass tube was immersed in liquid nitrogen by covering the quartz glass tube with liquid nitrogen for 3 minutes, and CO was added₂The gas is transferred from the cold finger S4 to the quartz glass tube through a pipeline;

s220, introducing pure carbon dioxide gas stored in the round-bottom flask 2 with the cold fingers into a quartz glass tube in sequence:

1) vacuumizing the whole system: by opening a control valve V3, a control valve V4 and a control valve V5, closing the control valve V1, the control valve V2-1-1, the control valve V2-1-2, the control valve V2-2-1, the control valve V2-2-2, the control valve V2-3-1, the control valve V2-3-2, the control valve V2-4-1, the control valve V2-4-2, the control valve V6, the control valve V7, the control valve V8 and the control valve V9; by means of a control valve V₄Vacuumizing the connected low-vacuum vacuumizing equipment until the vacuum is reduced to 10^-2mbar closes control valve V4, activatesThe high vacuum pumping equipment connected with the control valve V8 pumps vacuum to 10^-6mbar, continuously pumping for more than 30 minutes under the vacuum condition to ensure that the vacuum of the pipeline is clean;

2) gas transfer: then closing a control valve V5 and a control valve V8, sleeving liquid nitrogen at the position of a U-shaped cold trap S2, opening a control valve V2-2-1 on a round-bottom flask 2 with cold fingers, closing the control valve V2-2-1 after a period of time (preferably about 3 seconds), and opening a control valve V2-2-2; CO between control valve V2-2-1 and control valve V2-2-2₂The gas is transferred into a U-shaped cold trap S2 due to temperature difference, and the whole transfer time is about 5 minutes; ensuring pipeline CO₂After all the gas is absorbed, opening the control valve V5 and the control valve V8, pumping out impurity gas by using high-vacuum pumping equipment, and closing the control valve V5 and the control valve V8 after a period of time (about 2 minutes later); then covering liquid nitrogen on the cold finger S4, replacing the liquid nitrogen on the U-shaped cold trap S2 position sleeve with a mixture of methanol and liquid nitrogen at the temperature of-90 ℃ (note: analytical pure methanol is continuously added into the liquid nitrogen, stirring is carried out while adding, temperature is measured by temperature and temperature is adjusted to-90 ℃), a control valve V5 is opened, and CO is measured by a temperature sensor₂Transferring the gas from the U-shaped cold trap S2 to the cold finger S4, and keeping water in the U-shaped cold trap S2 to remove water in the carbon dioxide gas, closing the control valve V5 after the transfer is finished, and removing a mixture of methanol and liquid nitrogen at the temperature of-90 ℃ in the U-shaped cold trap S2; the liquid nitrogen in the cold finger S4 was changed to a mixture of methanol and liquid nitrogen at-90 deg.C, and the CO was read by a display instrument P2₂The amount of gas was measured, then the quartz glass tube was immersed in liquid nitrogen by covering the quartz glass tube with liquid nitrogen and opening the control valve V7 for 3 minutes, CO₂The gas is transferred from the cold finger S4 to the quartz glass tube through a pipeline;

s230, repeating the step S220 to respectively guide pure carbon dioxide gas stored in the round-bottom flask 3 with the cold fingers and the round-bottom flask 4 with the cold fingers into the quartz glass tube in sequence;

the difference is that when pure carbon dioxide gas stored in round-bottomed flask 3 with cold fingers is introduced into quartz glass tubes in sequence, liquid nitrogen is sleeved on U-shaped cold trap S2 in step 2), and control valve V2-3-1 on round-bottomed flask 3 with cold fingers is opened (instead of opening control valve on round-bottomed flask 2 with cold fingers)Valve V2-2-1), closing control valve V2-3-1 (instead of control valve V2-2-1) after a period of time (preferably about 3 seconds), opening control valve V2-3-2; CO between the control valve V2-3-1 and the control valve V2-3-2 (instead of between the control valve V2-2-1 and the control valve V2-2-2)₂The gas is transferred into a U-shaped cold trap S2 due to temperature difference, and the whole transfer time is about 5 minutes;

when pure carbon dioxide gas stored in the round-bottomed flask 4 with the cold fingers is sequentially introduced into the quartz glass tubes, in the step 2), liquid nitrogen is sleeved on the position of the U-shaped cold trap S2, the control valve V2-4-1 on the round-bottomed flask 4 with the cold fingers is opened (instead of opening the control valve V2-2-1 on the round-bottomed flask 2 with the cold fingers), the control valve V2-4-1 (instead of the control valve V2-2-1) is closed after a period of time (preferably about 3 seconds), and the control valve V2-3-2 is opened; CO between the control valve V2-4-1 and the control valve V2-4-2 (rather than between the control valve V2-2-1 and the control valve V2-2-2)₂The gas is transferred into a U-shaped cold trap S2 due to temperature difference, and the whole transfer time is about 5 minutes;

s240, sealing the upper end of the quartz glass tube by high-temperature fusion by using high-temperature flame (for example, more than 1000 ℃);

S300, balancing gas: sealing the tube well with CO₂The quartz glass tube is put into a muffle furnace at 1000 ℃ for 2-3 days to reach equilibrium (preferably 2 days), and then is rapidly cooled to room temperature to be measured;

wherein preferably the quartz glass tube encapsulates the CO₂The gas is firstly baked in a muffle furnace at 1000 ℃ for 2-3 hours before the gas is dried, and the step can effectively avoid packaging CO in a quartz glass tube₂Placing the gas in a muffle furnace at 1000 ℃ for cracking;

s410, connecting a quartz glass tube with the following process: the glass breaking device (Cracker) C1 was connected to the process via an external branch S3, and CO was introduced₂The well balanced quartz glass tube is connected to a glass crushing device C1, and the low vacuum pumping equipment is connected with an external branchThe path S5 is connected to the process, and the high vacuum pumping equipment is connected to the process through an external branch S7; wherein the quartz glass tube is not broken for a while;

s420, vacuumizing the whole system: under the condition that the quartz glass tube is not broken temporarily, the control valve V is closed₃Control valve V₆Control valve V₈Control valve V₉Opening the control valve V₄Control valve V₅Control valve V₇Vacuumizing by using low-vacuum vacuumizing equipment until the vacuum is reduced to 10^-2mbar cut-off control valve V₄Starting the control valve V₈The connected high vacuum-pumping equipment is vacuumized to 10^-6mbar；

S430, gas transfer: closing the control valve V₅Control valve V₈Breaking the seal of quartz glass tube by glass breaking device, covering liquid nitrogen on cold finger S4, covering mixture of methanol and liquid nitrogen at-90 deg.C on quartz glass tube, and introducing CO into quartz glass tube₂Transferring to a cold finger S4, and opening a control valve V after the transfer is completed₈Removing the miscellaneous gases, and then closing the control valve V₇Control valve V₈The liquid nitrogen on the cold finger S4 sleeve is changed into a mixture of methanol and liquid nitrogen at the temperature of-90 ℃, and CO is read by a pressure display instrument P2₂The amount of gas, and then the control valve V₆CO in cold finger S4₂The gas is transferred to the purification process of cluster gas, and the purified clean CO is obtained₂Collecting gas with special gas collecting bottle, injecting sample via two-way system of Mat-253, and testing delta_47-rawValue, here not expanded.

The principle and the implementation mode of the invention are explained by applying specific embodiments in the invention, and the description of the embodiments is only used for helping to understand the method and the core idea of the invention; meanwhile, for a person skilled in the art, according to the idea of the present invention, there may be variations in the specific embodiments and the application scope, and in summary, the content of the present specification should not be construed as a limitation to the present invention.

Claims

1. An apparatus for preparing a balance gas in a carbonate cluster isotope test, the apparatus comprising:

a control valve for controlling the on-off of each branch is arranged on the parallel branch of each carbon dioxide storage device; a connecting pipeline between the condensing devices is provided with a balance device external branch with a control valve; a purification system external branch with a control valve is arranged on a serial pipeline which is connected in series with the condensing equipment in sequence after the carbon dioxide storage equipment is connected in parallel, and the external branch is used for connecting a carbonate cluster isotope test purification system; at least one vacuumizing device external branch with a control valve is arranged on a serial pipeline which is connected in parallel with the carbon dioxide storage devices and then sequentially connected in series with the condensing device;

wherein, a series pipeline which is connected in parallel with the carbon dioxide storage devices and then connected in series with the condensing device in sequence is provided with a carbon dioxide source external branch with a control valve; or; the external branch of the balance equipment with the control valve can also be used for realizing the connection with a carbon dioxide gas source.

2. The apparatus of claim 1, wherein the condensing device comprises a cold trap and/or a cold finger.

3. The device according to claim 1, wherein at least two external branches of the vacuum extractor with control valves are arranged on a serial pipeline which is connected with the carbon dioxide storage equipment in series in sequence after being connected in parallel and is connected with the condensing equipment in series; at least one external branch of the vacuumizing device with a control valve is arranged in front of the condensing equipment, and at least one external branch of the vacuumizing device with a control valve is arranged behind the condensing equipment.

4. The apparatus of claim 1, wherein the apparatus is further provided with a pressure gauge, which is provided on a serial pipe connected in parallel to each carbon dioxide storage device and then connected in series to the condensing device, and/or on an external branch of the purification system with a control valve.

5. The apparatus of claim 4, wherein at least one pressure gauge is disposed adjacent to the balance apparatus external branch with the control valve.

6. The apparatus of claim 1, wherein,

the balance gas preparation device in the carbonate cluster isotope test further comprises a glass crushing device;

the balance gas preparation device in the carbonate cluster isotope test further comprises balance equipment, and the balance equipment is a glass tube.

7. The apparatus of claim 1, wherein each of the parallel branches of each carbon dioxide storage device is provided with at least two control valves for controlling the switching of the branches.

8. The apparatus of claim 1, wherein,

the pipeline used in the balance gas preparation device in the carbonate cluster isotope test selects a glass pipe or a stainless pipe pipeline with the inner wall polished;

the carbon dioxide storage equipment is storage equipment with a cold finger.

9. A method for preparing an equilibrium gas in a carbonate cluster isotope test, which is performed using the apparatus for preparing an equilibrium gas in a carbonate cluster isotope test described in any one of claims 1 to 8, wherein the method comprises:

10. The method of claim 9, wherein the step of conducting the pure carbon dioxide gas to a freezing dehydration and impurity removal device and then to an equilibrium device sequentially by using a condensing device based on the control of each control valve comprises:

D. the balance equipment is arranged in an environment capable of realizing carbon dioxide solidification, the environment where the last condensing equipment is located is adjusted to the environment capable of realizing carbon dioxide gasification and maintaining water in a solidification state from the environment capable of realizing carbon dioxide solidification, the pure carbon dioxide gas is transferred into the balance equipment and solidified, and water is still remained in the last original condensing equipment in the carbon dioxide gas transfer process to realize carbon dioxide gas dehydration.

11. The method of claim 10, wherein the last condensing device is a cold finger.

12. The method according to claim 9, wherein, in the step 2), deionized water is filled in the balancing device during the process of connecting the balancing device into the balanced gas preparation device in the carbonate cluster isotope test through the corresponding external branch, and the product obtained in the step 3) is water balanced gas.

13. The method of claim 9, wherein directing the equilibrated gas from the equilibration device out through a purification system external branch having a control valve into a carbonate cluster isotope testing purification system comprises:

G. the environment of the condensing equipment containing the balance gas is adjusted from the environment capable of realizing carbon dioxide solidification to the environment capable of realizing carbon dioxide gasification and maintaining water in a solidification state, the balance gas is led out to the carbonate cluster isotope test purification system by combining the control of each control valve, and water still remains in the condensing equipment in the process of leading out the balance gas to realize water removal.

14. The method of claim 10 or 13, wherein the environment capable of effecting solidification of carbon dioxide is a liquid nitrogen environment.

15. The method according to claim 10 or 13, wherein the environment capable of achieving carbon dioxide gasification and maintaining water in a solidified state is a mixture environment of methanol and liquid nitrogen at-90 ℃.

16. The method of claim 9, wherein the step 3) of achieving the balance of the components in the balancing device at the set temperature is achieved by:

wherein the set temperature is one of 1000 ℃, 50 ℃ and 15 ℃;

wherein the set period of time is not less than 2 hours.